X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (5372) 5372
Book / eBook (616) 616
Publication (389) 389
Magazine Article (63) 63
Book Chapter (38) 38
Book Review (38) 38
Newspaper Article (10) 10
Web Resource (6) 6
Newsletter (5) 5
Conference Proceeding (4) 4
Dissertation (4) 4
Data Set (3) 3
Reference (1) 1
Trade Publication Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (4245) 4245
male (2459) 2459
female (2402) 2402
teeth (1664) 1664
child (1564) 1564
index medicus (1308) 1308
adolescent (1137) 1137
adult (1131) 1131
dentistry (1054) 1054
dentistry, oral surgery & medicine (990) 990
animals (732) 732
tooth abnormalities - pathology (671) 671
radiography (670) 670
incisor - abnormalities (664) 664
child, preschool (655) 655
mutation (479) 479
middle aged (436) 436
stomatognathic system (421) 421
pathology (420) 420
stomatognathic diseases (413) 413
diagnosis (410) 410
surgery (410) 410
syndrome (379) 379
maxilla (374) 374
research (366) 366
mice (361) 361
tooth (352) 352
tooth root - abnormalities (351) 351
diseases (350) 350
phenotype (340) 340
mouth (327) 327
genetics & heredity (305) 305
tooth abnormalities (300) 300
abnormalities (299) 299
care and treatment (295) 295
tooth diseases (295) 295
infant (293) 293
pedigree (288) 288
prevalence (286) 286
follow-up studies (285) 285
mandible (285) 285
molar - abnormalities (281) 281
children (273) 273
clinical neurology (269) 269
incisor - pathology (269) 269
young adult (267) 267
tooth abnormalities - genetics (258) 258
charcot-marie-tooth disease - genetics (254) 254
case report (250) 250
molar - pathology (248) 248
orthodontics (245) 245
tooth abnormalities - diagnostic imaging (242) 242
charcot-marie-tooth disease (240) 240
bicuspid - abnormalities (224) 224
genetic aspects (223) 223
neurosciences (223) 223
tooth, deciduous - abnormalities (223) 223
medicine (219) 219
article (218) 218
tooth abnormalities - etiology (215) 215
disease (212) 212
tooth eruption (212) 212
dental enamel - abnormalities (211) 211
dentition (209) 209
pediatrics (208) 208
charcot-marie-tooth disease - pathology (207) 207
radiography, panoramic (207) 207
analysis (206) 206
diagnosis, differential (206) 206
enamel (200) 200
patients (198) 198
tooth extraction (195) 195
cuspid - pathology (190) 190
health aspects (189) 189
mouth diseases (189) 189
aged (186) 186
marie-tooth-disease (181) 181
tooth abnormalities - complications (175) 175
gene (174) 174
risk factors (174) 174
tooth, deciduous - pathology (174) 174
tooth, supernumerary - pathology (173) 173
cephalometry (172) 172
tooth - pathology (169) 169
abnormalities, multiple - pathology (164) 164
case studies (164) 164
maxilla - pathology (163) 163
mutations (161) 161
research article (160) 160
retrospective studies (159) 159
infant, newborn (156) 156
genetics (154) 154
proteins (150) 150
dental pulp cavity - abnormalities (147) 147
dents (145) 145
abnormalities, multiple - genetics (144) 144
age (144) 144
dental enamel - pathology (143) 143
expression (143) 143
mandible - pathology (141) 141
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
UTL at Downsview - May be requested (351) 351
Dentistry (Harry R Abbott) - Stacks (169) 169
Dentistry (Harry R Abbott) - May be requested in 6-10 wks (116) 116
Dentistry (Harry R Abbott) - Withdrawn (109) 109
Gerstein Science - Stacks (59) 59
Collection Dvlpm't (Acquisitions) - Closed Orders (20) 20
UofT at Mississauga - Stacks (10) 10
Dentistry (Harry R Abbott) - May be requested (9) 9
Collection Dvlpm't (Acquisitions) - Vendor file (8) 8
Dentistry (Harry R Abbott) - Circulation Desk (8) 8
Online Resources - Online (8) 8
Robarts - Stacks (5) 5
UofT at Scarborough - Stacks (5) 5
Dentistry (Harry R Abbott) - Mending (3) 3
Dentistry (Harry R Abbott) - Course Reserves (2) 2
Dentistry (Harry R Abbott) - Missing (2) 2
Dentistry (Harry R Abbott) - Rare Book (2) 2
Royal Ontario Museum - Stacks (2) 2
Scarborough Hospital - General (2) 2
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (2) 2
Dentistry (Harry R Abbott) - Searching (1) 1
Gerstein Science - Circulation Desk (1) 1
Gerstein Science - Missing (1) 1
Holland Bloorview Kids Rehabilitation - Stacks (1) 1
Lakeridge Health Sciences - Oshawa (1) 1
Providence Healthcare - Stacks (1) 1
Royal Ontario Museum - Periodical Stacks (1) 1
Scarborough Hospital - Birchmount (1) 1
St. Michael's Hospital - Stacks (1) 1
Thomas Fisher Rare Book - Rare Book (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (5632) 5632
French (115) 115
German (78) 78
Spanish (67) 67
Japanese (61) 61
Italian (54) 54
Russian (22) 22
Dutch (18) 18
Arabic (15) 15
Polish (12) 12
Portuguese (11) 11
Chinese (8) 8
Danish (8) 8
Croatian (7) 7
Turkish (7) 7
Hungarian (6) 6
Romanian (6) 6
Norwegian (4) 4
Czech (3) 3
Greek (3) 3
Swedish (3) 3
Bulgarian (2) 2
Slovak (2) 2
Afrikaans (1) 1
Finnish (1) 1
Korean (1) 1
Latvian (1) 1
Persian (1) 1
Slovenian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The American Journal of Human Genetics, ISSN 0002-9297, 10/2017, Volume 101, Issue 4, pp. 552 - 563
The Sonic Hedgehog (SHH) pathway is a key signaling pathway orchestrating embryonic development, mainly of the CNS and limbs. In vertebrates, SHH signaling is... 
polymicrogyria | developmental defects | hypomorphic variants | congenital ataxia | ciliopathies | SUFU | Joubert syndrome | Sonic Hedgehog | molar tooth sign | GLI3 | SHH | SIGNALING PATHWAY | GENETICS & HEREDITY | PLANAR CELL POLARITY | CEREBELLAR DEVELOPMENT | GLI PROTEINS | MUTATIONS | KIF7 | MEDULLOBLASTOMA | PHENOTYPIC SPECTRUM | PRIMARY CILIA | Abnormalities, Multiple - pathology | Skin - metabolism | Humans | Zinc Finger Protein Gli3 | Hedgehog Proteins - metabolism | Male | Bone Diseases, Developmental - genetics | Mutation, Missense | Cerebellum - abnormalities | Bone Diseases, Developmental - pathology | Gene Expression Regulation, Developmental | Kruppel-Like Transcription Factors - metabolism | Kidney Diseases, Cystic - genetics | Craniofacial Abnormalities - pathology | Female | Child | Abnormalities, Multiple - genetics | Craniofacial Abnormalities - genetics | Repressor Proteins - metabolism | Skin - pathology | Fibroblasts - metabolism | Repressor Proteins - chemistry | Signal Transduction | Cells, Cultured | Repressor Proteins - genetics | Eye Abnormalities - genetics | Fibroblasts - pathology | Genes, Recessive | Sequence Analysis, DNA | Cerebellum - pathology | Kidney Diseases, Cystic - pathology | Nerve Tissue Proteins - metabolism | Eye Abnormalities - pathology | Retina - abnormalities | Retina - pathology | Cohort Studies | Embryonic development | Usage | Gene mutations | Analysis | Nucleotide sequencing | Research | Diagnosis | Children | Health aspects | DNA sequencing
Journal Article
ZOOLOGICAL SCIENCE, ISSN 0289-0003, 08/2017, Volume 34, Issue 4, pp. 295 - 299
This study proposes a simple standardized method for the production of analog X-ray images of dolphin teeth, and to explore its potential use as a... 
CETACEA DELPHINIDAE | ZOOLOGY | X-rays | pulp stones | teeth | Cetacea | TURSIOPS-TRUNCATUS | dental wear | INIA-GEOFFRENSIS | Tooth Diseases - veterinary | Tooth Diseases - pathology | Radiography, Dental - veterinary | Animals | Tooth Diseases - diagnostic imaging | Dolphins
Journal Article
Zoological Science, ISSN 0289-0003, 08/2017, Volume 34, Issue 4, pp. 295 - 299
This study proposes a simple standardized method for the production of analog X-ray images of dolphin teeth, and to explore its potential use as a... 
Journal Article
Nature Genetics, ISSN 1061-4036, 04/2000, Volume 24, Issue 4, pp. 391 - 395
Journal Article
Journal Article
Journal Article
Genome Biology, ISSN 1474-7596, 2015, Volume 16, Issue 1, p. 293
BACKGROUND: Joubert syndrome (JBTS) and related disorders are defined by cerebellar malformation (molar tooth sign), together with neurological symptoms of... 
KIAA0556 | Joubert syndrome | Katanin | K04F10.2 | Microtubule | Basal body | Cilia | PROTEIN | PRIMARY CILIUM | FLAGELLAR LENGTH CONTROL | CAENORHABDITIS-ELEGANS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | CILIOPATHY | MUTATIONS | CILIOGENESIS | INTRAFLAGELLAR TRANSPORT | MOLECULAR-BASIS | Abnormalities, Multiple - pathology | Microtubule-Associated Proteins - genetics | Microtubule-Associated Proteins - metabolism | Humans | Child, Preschool | Male | Cerebellum - abnormalities | Brain - metabolism | Exome | Microtubules - metabolism | Basal Bodies - pathology | Kidney Diseases, Cystic - genetics | Adult | Female | ADP-Ribosylation Factors - metabolism | Child | Abnormalities, Multiple - genetics | Caenorhabditis elegans - metabolism | Cilia - pathology | Caenorhabditis elegans - genetics | Mice, Inbred C57BL | Cells, Cultured | Adenosine Triphosphatases - metabolism | Eye Abnormalities - genetics | Basal Bodies - metabolism | Cerebellum - pathology | Cilia - genetics | Kidney Diseases, Cystic - pathology | Animals | Eye Abnormalities - pathology | Pedigree | Retina - abnormalities | Brain - pathology | Protein Binding | Mice | Mutation | Retina - pathology | Cerebellum | Brain | Phenotypes | Nuclear magnetic resonance--NMR | Kidneys | Disease | Congenital defects | Teeth | Neurodevelopmental disorders | Defects | Proteins | Microtubules | Fibroblasts | Nematodes | Growth hormones | Research
Journal Article
Biochemical Journal, ISSN 0264-6021, 11/2015, Volume 472, Issue 1, pp. 55 - 69
Oculodentodigital dysplasia (ODDD) is primarily an autosomal dominant disorder linked to over 70 GJA1 gene [connexin43 (Cx43)] mutations. For nearly a decade,... 
Connexin43 | Extracellularmatrix | Oculodentodigital dysplasia | Fibroblast | Gap junctional intercellular communication | Collagen | CONNEXIN-43 HEMICHANNELS | connexin43 | NEUROLOGICAL MANIFESTATIONS | oculodentodigital dysplasia | COLLAGEN GEL CONTRACTION | BIOCHEMISTRY & MOLECULAR BIOLOGY | collagen | DOWN-REGULATION | FUNCTIONAL-CHARACTERIZATION | GAP-JUNCTION PROTEIN | CARDIAC FIBROBLASTS | MUTATIONS CAUSE | fibroblast | INTERCELLULAR COMMUNICATION | gap junctional intercellular communication | CENTRAL-NERVOUS-SYSTEM | extracellular matrix | Tooth Abnormalities - metabolism | Humans | Foot Deformities, Congenital - genetics | Foot Deformities, Congenital - metabolism | Immunoblotting | Syndactyly - pathology | RNA Interference | Craniofacial Abnormalities - pathology | Cell Culture Techniques | Craniofacial Abnormalities - metabolism | Eye Abnormalities - metabolism | Craniofacial Abnormalities - genetics | Connexin 43 - genetics | Disease Models, Animal | Fibroblasts - metabolism | Foot Deformities, Congenital - pathology | Tooth Abnormalities - genetics | Connexin 43 - metabolism | Syndactyly - metabolism | Cells, Cultured | Gene Expression Regulation | Eye Abnormalities - genetics | Reverse Transcriptase Polymerase Chain Reaction | Microscopy, Confocal | Animals | Eye Abnormalities - pathology | Tooth Abnormalities - pathology | Dermis - pathology | Mice | Mutation | Syndactyly - genetics
Journal Article